Portsmouth CORE-D Routine Care Data Repository
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16+
SponsorPortsmouth Hospitals NHS Trust
About this trial
An integrated database of depersonalised routine hospital patient data consisting of demographic and disease attributes, physiological or laboratory measurements, care contacts and interventions along with associated clinical outcomes. The database is an essential resource for the development and testing of risk models and classification systems, modified as necessary for patient subgroups, which can then be introduced into clinical care to improve patient outcomes. It can also be used for large scale simulations to evaluate interventions.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult presenting at the acute hospital or receiving services from the hospital
Disqualifiers
Adults who have registered an opt out of research with National Health Service (NHS) Digital
Adults who have contacted the hospital to ask that their records are not to be included in this study
Trial population
The research database will hold data on adults who are treated by Portsmouth Hospitals University National Health Service Trust (PHU), either as an outpatient, Accident and Emergency (A\&E) attender, day case or inpatient or have investigations carried out by PHU services Adult patients are defined by the National Health Service (NHS) as individuals over 16 years old. Data on service contacts and use will only be included where the patient was more than 16 years old at that time. None of the data included in the Clinical Outcomes analyses are collected specifically for the purposes of research. All datasets are routinely collected clinical datasets, collected for clinical use and clinical audit.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
In-hospital death
Death during hospital admission
Time frame
At 24 hours after an observation assessment or physiological measurement2
In-hospital death
Death during hospital admission
Time frame
30 days after admission3
Unanticipated ICU admission
Unanticipated ICU admission during hospital stay
Time frame
At 24 hours after an observation assessment or physiological measurement4
Unanticipated ICU admission
Unanticipated ICU admission during hospital stay
Time frame
30 days after admissionSecondary outcomes
1
Diagnosis of Corona Virus Disease (COVID) infection
Diagnosis of COVID-19
Time frame
48 hours after presentation2
Diagnosis of Corona Virus Disease (COVID) infection
Diagnosis of COVID-19
Time frame
At 48 hours after an observation assessment or physiological measurement3
Detection of Acute Organ Dysfunction
Detection of acute organ dysfunction as measured by components of the Sequential Organ Failure Assessment (SOFA) Score
Time frame
24 hours after presentation4
Detection of Acute Organ Dysfunction
Detection of acute organ dysfunction as measured by components of the Sequential Organ Failure Assessment (SOFA) Score
Time frame
48 hours after presentationSponsors and contacts
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Source ClinicalTrials.gov